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Analyst I, Postmarket Surveillance

Abbott

Burlington, MAJob$51–101K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$51–101K/yr
Location
Burlington, MA
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Bachelor's degree, required

Job overview

The Analyst I, Postmarket Surveillance role in Abbott’s Heart Failure Division analyzes customer complaints for regulatory reportability, compliance, and potential impact. The analyst investigates events, gathers information from clinical, field, internal, and laboratory sources, and prepares regulatory reports and customer communications. The position also supports event coding and complaint decision models, working with internal teams under supervisor guidance.

Skills & qualifications

RequiredNice to have

Skills

Complaint Assessment, nice to haveComplaint Investigation, nice to haveRegulatory Reportability, nice to haveRegulatory Reporting, nice to haveEvent Coding, nice to haveWritten Communication, nice to have

Qualifications

Bachelor's in Biomedical or Related Field, required0-2 Years Related Work Experience, required

Benefits

Medical Insurance
401(k) Match
Tuition Assistance

Full job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

The Opportunity

This position works out of our Burlington, MA location in the Heart Failure Division. In Abbott’s Heart Failure (HF) business, we’re developing solutions to diagnose, monitor and manage heart failure, allowing people to restore their health and get on with their lives.

This role analyzes customer complaints to determine which are regulatory reportable and coordinates activities with internal, field, and end use customers. Responsible for adherence to Good Manufacturing Practices (GMPs) and proper complaint handling per the Code of Federal Register (CFR) and other governmental regulations. Communicates event investigation results via regulatory reports and written communications, as appropriate.

What You’ll Work On

  • Review complaint communications and assess for regulatory compliance, reportability, and potential impact to patient safety and business operations.

  • Participate in development and modification of these decision models with changes in product advances/therapies to uphold consistent compliance with government-mandated regulations.

  • Evaluate and investigate identified complaints by gathering sufficient data from clinical staff, field representatives, internal employees, and laboratory analysis.

  • Collect, compile, and document regulatory reportability decisions using event investigation and regulatory decision models.

  • Draft Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities.

  • Apply codes to events to facilitate product performance records.

  • Review coding and investigations with engineering, laboratory, and other internal staff.

  • Draft written communications detailing the clinical observation, investigation and/or product analysis, and corrective actions, as applicable, to physician and other end use customers.

  • Communications include determination/eligibility for warranty credit or unreimbursed medical payments.

  • Begins establishing and cultivating a network of internal resources to facilitate completion of tasks.

  • Individual influence is typically exerted at the peer level.

  • Completes daily work to meet established schedule with guidance from supervisor on prioritization of tasks.

  • May exercise authority within pre-established limits and approval.

  • Failure to achieve results can normally be overcome without serious effect on the business.

Required Qualifications

  • Bachelor's degree in biomedical or related field

  • 0-2 years of related work experience

Apply Now (https://www.jobs.abbott/us/en)

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott , and on Twitter @AbbottNews.

The base pay for this position is $50,700.00 – $101,300.00. In specific locations, the pay range may vary from the range posted.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email [email protected]

How this job compares

Set against the 1,020 open Regulatory Affairs jobs on Olive Jobs, counted November 12, 2026.

Pay
  • This posting$51–101K/yr
  • Massachusetts median$137–185K/yr55 salary ranges
  • US median$140–203K/yr688 salary ranges

This range's midpoint, $76K, is 53% below the Massachusetts median midpoint ($162K) — in the lowest quarter of Regulatory Affairs salary ranges in Massachusetts.

Openings
Olive Jobs lists 64 open Regulatory Affairs jobs in Massachusetts and 1,020 across the US. 17% of them nationwide are listed as remote or flexible.
Hiring the most in Massachusetts
Experience
This posting asks for no prior experience — less than three in four Regulatory Affairs postings that state a minimum ask for (median 7 years, across 891 postings).
Education
This posting asks for a bachelor's degree; 607 of the 1,020 open Regulatory Affairs jobs (60%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 12, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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